Liposomal irinotecan + 5-fluorouracil + leucovorin + bevacizumab as second-line therapy in metastatic colorectal cancer (IRIS): A multi-center, single-arm, prospective, phase II study.

X Xuhua Hu B Bo Jiang (Chinese Education Ministry Key Lab and Joint International Research Lab of Resource Chemistry, Shanghai Frontiers Science Center of Biomimetic Catalysis, College of Chemistry and Materials Science) L Lu Hongxia (Shanxi Tumor Hospital, Taiyuan, China) B Bin Yu B Bo Yi (Department of Chemistry and Biotechnology Graduate School of Engineering The University of Tokyo 7‐3‐1 Hongo, Bunkyo‐ku Tokyo 113‐8656 Japan) Y YuDong Wang L Lingjun Zhu (State Key Laboratory of Precision and Intelligent Chemistry, Department of Chemical Physics) S Shengmian Li (Department of Gastroenterology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China) B Baokun Li D Dalu Kong Z Zhiwu Wang W Wenbo Niu H Hongqing Ma S Shanchuan Wang (Shanxi Cancer Hospital, Taiyuan, Shanxi, China) Y Yanglin Chen (Jiangxi Cancer Hospital, Nanchang, Jiangxi, China) C Chao Lin R Rong Yang W Weiyou Zhu (Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China) J Jia Liu G Guiying Wang

Abstract

195 Background: In patients with advanced colorectal cancer (CRC), the recommended second-line treatment following first-line therapy with oxaliplatin-based regimens is irinotecan-based therapy. Liposomal irinotecan, a novel formulation of traditional irinotecan, has demonstrated potential to enhance efficacy while minimizing toxicity. This study aims to investigate the efficacy and safety of liposomal irinotecan in combination with 5-FU/LV and bevacizumab as a second-line treatment option for metastatic CRC. Methods: This is a multi-center, single-arm, prospective, phase II study. Patients with metastatic CRC who received oxaliplatin-based chemotherapy as first-line treatment were enrolled to receive liposomal irinotecan + 5-fluorouracil + leucovorin + bevacizumab regimen until disease progression and/or unacceptable toxicity. The primary endpoint is objective response rate (ORR), secondary endpoints include disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety. Results: A total of 50 patients were enrolled from Jan 2024 to Jul 2024 across 6 sites in China. The median age was 56.5 years (range: 30.0-76.0), with 58.0% male and 36.0% ECOG 0. Among the patients, 38.0% had left-sided colon cancer, 24.0% had right-sided colon cancer, and 38.0% had rectal cancer. As of Sept 14, 2024, 39 patients had at least one tumor assessment and 19 patients were still on treatment. ORR and DCR were 20.5% (8/39, 95% CI: 9.3%-36.5%) and 84.6% (33/39, 95% CI: 69.5%-94.1%), respectively. Eleven patients had disease progression and 5 patients died, and the median PFS and OS were not reached. The relative dose intensity of liposomal irinotecan and 5-fluorouracil were 92.8% (range: 23.6%-109.6%) and 89.5% (range: 13.3%-116.8%), respectively. During treatment, 43 (86.0%) patients had at least one adverse event (AE) and 24 (48.0%) had grade 3-4 AE. Most common (≥ 10%) grade 3-4 AEs were neutropenia (20.0%), leukocytopenia (16.0%) and diarrhea (10.0%). No unexpected toxicities observed in this study. Conclusions: These preliminary results reveled that liposomal irinotecan + 5-fluorouracil + leucovorin + bevacizumab after oxaliplatin-based treatment for metastatic CRC was well tolerated with encouraging clinical activity, which warrants further follow up. Clinical trial information: NCT06184698 .

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 195-195
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

X

Xuhua Hu

B

Bo Jiang

Chinese Education Ministry Key Lab and Joint International Research Lab of Resource Chemistry, Shanghai Frontiers Science Center of Biomimetic Catalysis, College of Chemistry and Materials Science

L

Lu Hongxia

Shanxi Tumor Hospital, Taiyuan, China

B

Bin Yu

B

Bo Yi

Department of Chemistry and Biotechnology Graduate School of Engineering The University of Tokyo 7‐3‐1 Hongo, Bunkyo‐ku Tokyo 113‐8656 Japan

Y

YuDong Wang

L

Lingjun Zhu

State Key Laboratory of Precision and Intelligent Chemistry, Department of Chemical Physics

S

Shengmian Li

Department of Gastroenterology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China

B

Baokun Li

D

Dalu Kong

Z

Zhiwu Wang

W

Wenbo Niu

H

Hongqing Ma

S

Shanchuan Wang

Shanxi Cancer Hospital, Taiyuan, Shanxi, China

Y

Yanglin Chen

Jiangxi Cancer Hospital, Nanchang, Jiangxi, China

C

Chao Lin

R

Rong Yang

W

Weiyou Zhu

Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China

J

Jia Liu

G

Guiying Wang